
简介:
- 作者: Michal Guberman Bracha, Guy Biber Guy Biber, Natalie Zelikson, Sharon Shavit, Roy Avraham, Yaron Vagima, Débora Rosa Bublik, Yael Katz, Adi Barzel, Leah Natasha Klapper, Shmuel Hess, Alessio David Nahmad
- 杂志: Frontiers in Immunology
- Doi: https://www.doi.org/10.3389/fimmu.2025.1613879
- 出版日期: 2025-7-18
摘要
Transplantation of engineered B cells has demonstrated efficacy in HIV disease models. B cell engineering may also be utilized for the treatment of cancer. Recent studies have highlighted that B cell activity is associated with favorable clinical outcomes in oncology. In mice, polyclonal B cells have been shown to elicit anti-cancer responses. As a potential novel cell therapy, we demonstrate that engineering B cells to target a tumor-associated antigen enhances polyclonal anti-tumor responses. We observe that engineered B cells expressing an anti-HPV B cell receptor internalize the antigen, enabling subsequent activation of oncoantigen-specific T cells. Secreted antibodies from engineered B cells form immune complexes, which are taken up by antigen-presenting cells to further promote T cell activation. Engineered B cells hold promise as novel, multi-modal cell therapies and open new avenues in solid tumor targeting.
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